EP1719755A1 - Procédé et système pour la préparation d'urée - Google Patents

Procédé et système pour la préparation d'urée Download PDF

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Publication number
EP1719755A1
EP1719755A1 EP05009761A EP05009761A EP1719755A1 EP 1719755 A1 EP1719755 A1 EP 1719755A1 EP 05009761 A EP05009761 A EP 05009761A EP 05009761 A EP05009761 A EP 05009761A EP 1719755 A1 EP1719755 A1 EP 1719755A1
Authority
EP
European Patent Office
Prior art keywords
urea
section
ammonia
carbon dioxide
aqueous solution
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP05009761A
Other languages
German (de)
English (en)
Inventor
Federico Zardi
Paolo Sticchi
Paolo Brunengo
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Casale SA
Original Assignee
Urea Casale SA
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Urea Casale SA filed Critical Urea Casale SA
Priority to EP05009761A priority Critical patent/EP1719755A1/fr
Priority to RU2007144524/04A priority patent/RU2412163C2/ru
Priority to PCT/EP2006/003121 priority patent/WO2006117050A1/fr
Priority to CN2006800142538A priority patent/CN101166716B/zh
Priority to US11/911,461 priority patent/US7608735B2/en
Priority to BRPI0610894A priority patent/BRPI0610894B1/pt
Priority to CA2606357A priority patent/CA2606357C/fr
Priority to EP06742542.1A priority patent/EP1877368B1/fr
Priority to PL06742542T priority patent/PL1877368T3/pl
Priority to UAA200713409A priority patent/UA91363C2/ru
Priority to SA06270127A priority patent/SA06270127B1/ar
Publication of EP1719755A1 publication Critical patent/EP1719755A1/fr
Priority to EGNA2007001182 priority patent/EG25069A/xx
Withdrawn legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C273/00—Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
    • C07C273/02—Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups of urea, its salts, complexes or addition compounds
    • C07C273/04—Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups of urea, its salts, complexes or addition compounds from carbon dioxide and ammonia

Definitions

  • the present invention concerns a process for urea production from ammonia and carbon dioxide, made to react at a predetermined high pressure in an appropriate synthesis section.
  • the invention refers to a process of the aforementioned type in which the product of the ammonia/carbon dioxide reaction, essentially consisting of an aqueous solution comprising urea, ammonium carbamate and ammonia, is subjected to a high-pressure recovery step of the ammonium carbamate and of the ammonia, which are recycled to the synthesis section, whereas the urea aqueous solution is sent to a urea recovery section operating at a predetermined low pressure to obtain urea with the least possible amount of possible residues of ammonia and carbon dioxide.
  • the present invention concerns a process of the type considered, in which the aforementioned recovery of carbamate and ammonia comprises the steps of decomposition of the carbamate and stripping, preferably with a gaseous reactant (in particular CO 2 ), of the ammonia and carbon dioxide thus produced, in a respective stripping zone, subsequent recondensation, in a respective condensation zone, of said ammonia and carbon dioxide into carbamate that is recycled to the synthesis section and in which said steps, together with the urea synthesis reaction, are all carried out substantially at the same high pressure (for example 135-175 bar), constituting a loop called, in the technical field, "High Pressure Loop” or "High Pressure Synthesis Loop” (H.P. Loop).
  • a gaseous reactant in particular CO 2
  • the invention also refers to a plant for carrying out the aforementioned process.
  • such a medium pressure treatment section comprises a dissociation step followed by a stripping step with feed CO 2 of the aqueous solution comprising urea, ammonium carbamate and ammonia and a subsequent condensation step of the vapours (ammonia, CO 2 and water) thus obtained with the addition of feed ammonia and a carbamate aqueous solution (carbonate) coming from the low pressure urea recovery section.
  • the carbamate aqueous solution obtained from the medium pressure condensation step is then recycled to the high pressure synthesis loop (H.P. loop).
  • a process of this type is for example described in WO-A-02 909 323 or else in NL-A-8 900 152 .
  • the technical problem underlying the present invention is that of devising and providing a process for urea production of the type considered above, in which a high production capacity of the plant intended to carry it out can be achieved and at the same time that ensures a high conversion yield of the carbon dioxide to urea in an efficient manner and with low energy consumption, overcoming the aforementioned drawbacks with reference to the prior art.
  • the process according to the present invention also comprises the steps of:
  • said part of aqueous solution comprising urea, ammonium carbamate and ammonia fed to said treatment section operating at medium pressure is comprised between 10 and 50 wt.% of said aqueous solution comprising urea, ammonium carbamate and ammonia obtained in said synthesis section.
  • said medium pressure of the treatment section is comprised between 10 and 70 bar.
  • said recycle ammonium carbamate aqueous solution obtained in said condenser of the low pressure urea recovery section is fed to said condensation step of the vapour phase comprising ammonia, carbon dioxide and water in said treatment section.
  • said condensation step of the vapour phase comprising ammonia, carbon dioxide and water in said treatment section is of the double-effect type.
  • the process according to the present invention it has surprisingly and advantageously been found that the amount of condensation water (in absolute value) necessary to recycle the unreacted ammonia and the carbon dioxide in the form of ammonium carbamate to the synthesis section is substantially less with respect to the amount of condensation water (in absolute value) required to carry out such recycling with the processes according to the prior art, in which feed carbon dioxide and feed ammonia are fed to the medium pressure treatment section.
  • the present technical problem is solved by a plant for carrying out the aforementioned process, comprising a high-pressure urea synthesis section, a medium pressure treatment section of a part of the urea solution produced in said synthesis section, comprising a dissociator and a condenser, and a low pressure urea recovery section comprising a decomposer and a condenser, such sections being in fluid communication with each other, the plant being characterized in that it comprises a connection duct between said dissociator of the medium pressure treatment section and said decomposer of the low pressure urea recovery section.
  • the plant for urea production according to the aforementioned process can be a brand new plant or else can be obtained by modifying a pre-existing plant in order to increase its capacity.
  • a method for revamping a pre-existing plant for urea production from ammonia and carbon dioxide of the type comprising a high-pressure urea synthesis section and a low pressure urea recovery section comprising a decomposer and a condenser, such sections being in fluid communication with each other is provided which is characterized in that it comprises the steps of:
  • ammonia N and carbon dioxide C are fed into an appropriate synthesis section 11.
  • the urea synthesis section comprises a single reactor R.
  • the ammonia N is fed to the reactor R through a condenser 12 and the carbon dioxide C is in turn fed to the reactor R through a stripper 13 and the condenser 12.
  • the synthesis section 11 (reactor R), the condenser 12, the stripper 13, together with a scrubber 14 (that shall be described hereafter in greater detail), all operate substantially at the same high pressure, thus constituting the high pressure synthesis loop (H.P. Loop) of the process of the present invention.
  • the ammonia and carbon dioxide are made to react at the aforementioned predetermined high pressure (for example comprised between 130 and 170 bar) and at a predetermined high temperature (for example comprised between 160 and 200°C). From the reactor R an aqueous solution comprising urea, ammonium carbamate and ammonia is obtained.
  • a part of the aqueous solution comprising urea, ammonium carbamate and ammonia exiting the reactor R is suitably decompressed in a per se conventional way for example by means of a valve 15 and fed to a treatment section 16 of such an aqueous solution operating at a predetermined medium pressure, for example comprised between 10 and 70 bar, preferably comprised between 15 and 25 bar, and even more preferably comprised between 18-20 bar.
  • a predetermined medium pressure for example comprised between 10 and 70 bar, preferably comprised between 15 and 25 bar, and even more preferably comprised between 18-20 bar.
  • the part of aqueous solution comprising urea, ammonium carbamate and ammonia suitably decompressed is fed to a medium pressure dissociator 17 at the treatment section 16 and subjected to dissociation obtaining an urea aqueous solution and a vapour phase comprising ammonia, carbon dioxide and water.
  • a part of aqueous solution comprising urea, ammonium carbamate and ammonia is subjected in the dissociator 17 to thermal dissociation.
  • vapour phase comprising ammonia, carbon dioxide and water thus obtained is then fed and subjected to condensation in a medium pressure condenser 18 of the treatment section 16.
  • a medium pressure condenser 18 of the treatment section 16 an ammonium carbamate aqueous solution is obtained that exits the condenser 18 and is recycled to the urea synthesis section 11 (reactor R).
  • the carbamate aqueous solution exiting the medium pressure condenser 18 is suitably compressed in a per se conventional way for example by means of a pump 19 and recycled to the reactor R of the high pressure urea synthesis section 11 through the scrubber 14 and the high pressure condenser 12.
  • a pump 19 the carbamate aqueous solution exiting the medium pressure condenser 18 is fed, suitably compressed, directly to the high pressure condenser 12 to then flow into the reactor R.
  • the process for urea production advantageously foresees the further step of feeding the urea aqueous solution obtained by dissociation in the medium pressure dissociator 17 of the treatment section 16 to a decomposer 22 of a urea recovery section 21 operating at a predetermined low pressure, for example comprised between 1.5 and 9.5 bar, preferably comprised between 3 and 5 bar.
  • the urea aqueous solution exiting the dissociator 17 is suitably decompressed in a per se conventional way for example by means of a valve 20.
  • the urea aqueous solution exiting the dissociator 17 of the treatment section 16 is directly fed to the decomposer 22 of the urea recovery ,section 21.
  • a part of the feed carbon dioxide C is preferably and advantageously fed to a condenser 23 of the low pressure urea recovery section 21.
  • the urea aqueous solution coming from the dissociator 17 of the medium pressure treatment section 16 is subjected to decomposition obtaining a concentrated urea solution U and a second vapour phase comprising ammonia, carbon dioxide and water.
  • the concentrated urea solution U exits the decomposer 22 of the urea recovery section 21 to be subjected to the final urea treatment steps (per se conventional and therefore not represented) of the process for urea production, such as the vacuum decomposition step and the granulation or prilling step of the molten urea thus obtained.
  • the second vapour phase comprising ammonia, carbon dioxide and water obtained in the decomposer 22 of the urea recovery section 21 is, on the other hand, sent to the condenser 23 of the same section 21 and advantageously subjected to condensation obtaining a recycle carbamate aqueous solution.
  • the second vapour phase comprising ammonia, carbon dioxide and water is subjected to condensation together with the feed carbon dioxide C fed to said condenser 23.
  • a suitable amount of an carbamate aqueous solution (carbonate) having a condensation water content comprised between 40 and 80 wt.% is also fed to the condenser 23 of the low pressure urea recovery section 21, to allow the second vapour phase and the feed carbon dioxide C, respectively, to condense to ammonium carbamate.
  • the carbamate aqueous solution W (carbonate) generally comes from a treatment section of the process condensate and/or from an ammonia liquor reservoir, per se conventional and not represented in figure 1.
  • the recycle carbamate aqueous solution obtained in the condenser 23 of the low pressure urea recovery section 21 is, according to the present process, fed into the medium pressure condenser 18 of the treatment section 16 for the absorption (condensation) of the vapour phase comprising ammonia, carbon dioxide and water coming from the medium pressure dissociator 17.
  • the step of compressing the recycle carbamate aqueous solution exiting the condenser 23, to the operating pressure of the treatment section 16 is also foreseen in a per se conventional way for example by means of a pump 24.
  • the condensation step in the condenser 18 of the medium pressure treatment section 16 is of the double effect type, in which the condensation heat, instead of being dissipated in a cooling fluid (generally cooling water), is advantageously exploited to further concentrate the concentrated urea solution U exiting the decomposer 22 of the low pressure urea recovery section.
  • a cooling fluid generally cooling water
  • the condensation heat that develops during the condensation of the vapour phase is transmitted by indirect heat exchange to the concentrated urea solution U, allowing the decomposition and therefore the separation of a part of the ammonium carbamate, ammonia and water still present in such a solution and thus further concentrating the urea contained in it.
  • aqueous solution comprising urea, ammonium carbamate and ammonia, exiting the reactor R and not sent to the medium pressure treatment section 16, is subjected to the recovery phase of the ammonium carbamate and of the ammonia present in such a solution, in the high pressure loop of the present process.
  • the remaining part of the aqueous solution comprising urea, ammonium carbamate and ammonia exiting the reactor R of the synthesis section 11 is fed to the high pressure stripper where it is subjected to decomposition and stripping with feed carbon dioxide C.
  • the ammonia and carbon dioxide thus produced are then recondensed into ammonium carbamate in the high pressure condenser 12 and recycled in the form of ammonium carbamate to the reactor R of the urea synthesis section 11.
  • the condensation in the high pressure condenser 12 of the ammonia and carbon dioxide coming from the stripper 13 is made to occur by absorption of such gases with the feed ammonia N (liquid) and with the carbamate aqueous solution coming, suitably compressed, from the condenser 18 of the medium pressure treatment section 16, through the scrubber 14.
  • aqueous solution comprising urea, ammonium carbamate and ammonia obtained in the stripper 13 following the aforementioned decomposition and stripping steps with CO 2 is suitably decompressed in a per se conventional way for example by means of a valve 25 at the operating pressure of the urea recovery section 21 and fed to the low pressure decomposer 22 of such a section 21.
  • a solution is subjected to decomposition, together with said urea aqueous solution coming from the dissociator 17 of the medium pressure treatment section 16, obtaining the concentrated urea solution U and the second vapour phase comprising ammonia, carbon dioxide and water, described above.
  • vapour phase present in the urea synthesis section 11, or rather in the reactor R, are made to exit the latter and fed to the high pressure scrubber 14.
  • vapours generally also comprise inert gases (for example air) present in the feed carbon dioxide C:
  • the aforementioned vapours are subjected to a washing treatment with the carbamate aqueous solution coming, suitably compressed, from the condenser 18 of the medium pressure treatment section 16, for the recovery of the carbon dioxide and ammonia present in them and the separation of the inert gases.
  • the inert gases thus separated are then released into the atmosphere in a per se conventional manner, moreover foreseeing suitable decompression thereof for example by means of a valve 26.
  • such inert gases can be recycled in other parts of the plant (not represented).
  • the carbon dioxide and ammonia absorbed in the carbamate aqueous solution coming from the condenser 18 are, on the other hand, recycled to the urea synthesis section 11, or rather to the reactor R, through the high pressure condenser 12.
  • the part of aqueous solution comprising urea, ammonium carbamate and ammonia sent to the medium pressure treatment section 16 is preferably comprised between 10 and 50 wt.%, even more preferably comprised between 10 and 25 wt.%, of the aqueous solution coming from the urea synthesis section 11.
  • the plant 10 comprises a high pressure urea synthesis section 11, a medium pressure treatment section 16 and a low pressure urea recovery section 21 arranged in fluid communication with each other.
  • the treatment section 16 advantageously comprises a medium pressure dissociator 17 and a medium pressure condenser 18 in fluid communication with each other.
  • the urea recovery section 21 comprises a low pressure decomposer 22 and a low pressure condenser 23 in fluid communication with each other.
  • respective feed ducts are foreseen of the reactants, carbon dioxide C and ammonia N, and of an carbamate aqueous solution W (carbonate) comprising condensation water, as well as connection ducts between the different sections and the corresponding apparatuses, schematically represented in figure 1 by the different flow lines.
  • connection ducts 28 and 29 are advantageously foreseen for the direct connection between the urea synthesis section 11 and the dissociator 17 of the medium pressure treatment section 16, and between this apparatus and the decomposer 22 of the low pressure urea recovery section 21, respectively.
  • a duct 27 for feeding feed carbon dioxide C to the condenser 23 of the low pressure urea recovery section 21 is also foreseen.
  • the medium pressure condenser 18 comprises a conventional tube bundle, in fluid communication, on the inside, i.e. tube side, with the concentrated urea solution U exiting the low pressure decomposer 22, and in fluid communication, on the outside, i.e. shell side, with the vapour phase comprising ammonia, carbon dioxide and water coming from the medium pressure dissociator 17 as well as with the recycle carbamate aqueous solution coming from the low pressure condenser, to obtain the double effect described above.
  • the process for urea production according to the invention solves the technical problem and achieves numerous advantages the first of which lies in the fact that a high overall conversion yield is obtained in the high pressure loop, and in particular in the urea synthesis section, for example comprised between 58 and 62 wt.%, irrespective of the required production capacity of the plant provided to carry it out.
  • the claimed process is thus also particularly advantageous for high capacity plants, for example to produce between 3000 and 4500 Metric Ton/day of urea.
  • a further advantage is that, thanks to the present invention and in particular to the high conversion yield, it is possible to reduce the energy consumption of the high pressure synthesis loop as well as of the low pressure urea recovery section, with respect to the processes according to the prior art. It follows from this that with the same energy consumption and size of the apparatuses that constitute the plant for urea production, the process according to the present invention allows operation in such a plant with a higher production capacity with respect to what is allowed with the processes according to the prior art. In other words, with the same production capacity, the plant intended to carry out the process according to the present invention is smaller in size, and thus more cost-effective and with less operating costs, with respect to the plant necessary to obtain such a capacity with the methods of the prior art.
  • the actuation of the process is particularly simple and reliable, and does not require large investment costs.
  • condensation water is recycled to the urea synthesis section together with the ammonium carbamate and given that water is a reaction product in urea synthesis and that therefore has a negative influence upon the conversion of the reactants, the fact of managing to substantially reduce such an amount of condensation water has advantageously involved a corresponding increase in the conversion yield with respect to the processes according to the prior art.
  • the processes according to the prior art necessarily foresee, in the medium pressure treatment section 16, a stripping step with feed carbon dioxide of the urea aqueous solution previously obtained by thermal dissociation in such a section and a condensation step with the addition of feed ammonia.
  • a stripping step with feed carbon dioxide of the urea aqueous solution previously obtained by thermal dissociation in such a section and a condensation step with the addition of feed ammonia.
  • the aforementioned amount of condensation water contained in the carbamate aqueous solution W (carbonate) is 10-25 wt.% less with the process according to the present invention with respect to the prior art, with a corresponding increase in the conversion yield in the high pressure urea synthesis section of 2-3%.
  • the plant 10 for urea production is obtained from a revamping method (modernization) of a pre-existing plant for urea production from ammonia and carbon dioxide of the type comprising a high pressure urea synthesis section 11 and a low pressure urea recovery section 21 comprising a decomposer 22 and a condenser 23, such sections 11, 21 being arranged in fluid communication with each other, characterized in that it comprises the steps of:
  • the method according to the present invention foresees the further step of providing a duct 27 for feeding feed carbon dioxide C to said condenser 23 of the low pressure urea recovery section 21.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Seasonings (AREA)
EP05009761A 2005-05-04 2005-05-04 Procédé et système pour la préparation d'urée Withdrawn EP1719755A1 (fr)

Priority Applications (12)

Application Number Priority Date Filing Date Title
EP05009761A EP1719755A1 (fr) 2005-05-04 2005-05-04 Procédé et système pour la préparation d'urée
BRPI0610894A BRPI0610894B1 (pt) 2005-05-04 2006-04-06 processo para produção de uréia e planta relacionada
PCT/EP2006/003121 WO2006117050A1 (fr) 2005-05-04 2006-04-06 Procede de production d'uree et usine associee
CN2006800142538A CN101166716B (zh) 2005-05-04 2006-04-06 尿素生产方法和相关设备
US11/911,461 US7608735B2 (en) 2005-05-04 2006-04-06 Process for urea production and related plant
RU2007144524/04A RU2412163C2 (ru) 2005-05-04 2006-04-06 Способ и установка для получения мочевины
CA2606357A CA2606357C (fr) 2005-05-04 2006-04-06 Procede de production d'uree et usine associee
EP06742542.1A EP1877368B1 (fr) 2005-05-04 2006-04-06 Procéde de production d'urée et usine associée
PL06742542T PL1877368T3 (pl) 2005-05-04 2006-04-06 Sposób wytwarzania mocznika i stosowna instalacja
UAA200713409A UA91363C2 (ru) 2005-05-04 2006-04-06 Способ и установка для получения мочевины, а также способ реконструкции прежде смонтированной установки
SA06270127A SA06270127B1 (ar) 2005-05-04 2006-05-03 عملية لإنتاج اليوريا ووحدة إنتاج متعلقة بذلك
EGNA2007001182 EG25069A (en) 2005-05-04 2007-10-30 Process for urea production and related plant.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP05009761A EP1719755A1 (fr) 2005-05-04 2005-05-04 Procédé et système pour la préparation d'urée

Publications (1)

Publication Number Publication Date
EP1719755A1 true EP1719755A1 (fr) 2006-11-08

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Family Applications (2)

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EP05009761A Withdrawn EP1719755A1 (fr) 2005-05-04 2005-05-04 Procédé et système pour la préparation d'urée
EP06742542.1A Active EP1877368B1 (fr) 2005-05-04 2006-04-06 Procéde de production d'urée et usine associée

Family Applications After (1)

Application Number Title Priority Date Filing Date
EP06742542.1A Active EP1877368B1 (fr) 2005-05-04 2006-04-06 Procéde de production d'urée et usine associée

Country Status (11)

Country Link
US (1) US7608735B2 (fr)
EP (2) EP1719755A1 (fr)
CN (1) CN101166716B (fr)
BR (1) BRPI0610894B1 (fr)
CA (1) CA2606357C (fr)
EG (1) EG25069A (fr)
PL (1) PL1877368T3 (fr)
RU (1) RU2412163C2 (fr)
SA (1) SA06270127B1 (fr)
UA (1) UA91363C2 (fr)
WO (1) WO2006117050A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1918273A1 (fr) * 2006-11-04 2008-05-07 Urea Casale S.A. Procédé et installation pour la production d'urée

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2153880A1 (fr) * 2008-07-31 2010-02-17 Urea Casale S.A. Procédé et installation pour la production d'une solution d'urée à utiliser dans le procédé SCR pour la réduction de Nox
CN101624355B (zh) * 2009-08-10 2012-05-23 四川金象赛瑞化工股份有限公司 一种低水碳比-三段吸收-蒸发式氨冷的尿素生产中压回收工艺
EP2397463A1 (fr) * 2010-06-16 2011-12-21 Urea Casale SA Procédé de remaniement d'une installation de production d'urée à vaporisation autonome
EP2941416B1 (fr) * 2012-12-28 2017-09-06 Stamicarbon B.V. Procédé de transformation d´une installation de synthèse d'urée
EP3398935A1 (fr) * 2017-05-05 2018-11-07 Casale Sa Procédé et installation de synthèse de l'urée
CN113195449B (zh) * 2018-12-21 2022-05-24 斯塔米卡邦有限公司 在低压回收段具有热整合的尿素生产方法和装置
US11814340B2 (en) 2020-06-23 2023-11-14 Stamicarbon B.V. Thermal stripping urea plant and process

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4864059A (en) * 1984-11-02 1989-09-05 Toyo Engineering Corporation Process for producing urea
WO2002090323A1 (fr) * 2001-05-03 2002-11-14 Dsm Ip Assets B.V. Procede de preparation d'uree

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL8900152A (nl) 1989-01-23 1990-08-16 Stamicarbon Werkwijze voor de bereiding van ureum.

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4864059A (en) * 1984-11-02 1989-09-05 Toyo Engineering Corporation Process for producing urea
WO2002090323A1 (fr) * 2001-05-03 2002-11-14 Dsm Ip Assets B.V. Procede de preparation d'uree

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1918273A1 (fr) * 2006-11-04 2008-05-07 Urea Casale S.A. Procédé et installation pour la production d'urée
WO2008052639A1 (fr) * 2006-11-04 2008-05-08 Urea Casale S.A. Procédé destiné à produire de l'urée et installation associée
US7982068B2 (en) 2006-11-04 2011-07-19 Urea Casale S.A. Process for urea production and related plant

Also Published As

Publication number Publication date
UA91363C2 (ru) 2010-07-26
SA06270127B1 (ar) 2010-11-22
US7608735B2 (en) 2009-10-27
US20090124830A1 (en) 2009-05-14
EP1877368A1 (fr) 2008-01-16
PL1877368T3 (pl) 2016-03-31
BRPI0610894B1 (pt) 2016-01-26
EG25069A (en) 2011-07-27
RU2412163C2 (ru) 2011-02-20
BRPI0610894A2 (pt) 2010-08-03
EP1877368B1 (fr) 2015-10-14
CN101166716A (zh) 2008-04-23
CA2606357A1 (fr) 2006-11-09
CN101166716B (zh) 2012-02-15
CA2606357C (fr) 2013-08-06
WO2006117050A1 (fr) 2006-11-09
RU2007144524A (ru) 2009-06-10

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